iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6172731	snp	A/G	0.290657	0.246672	intron-variant	Huwe1	Mm_Celera	X:151920441	TTTCCAGACTATACA[A/G]TAATAGACTGAATGA	59026
rs6172894	snp	G/T	0.495	0.0497494	intron-variant	Huwe1	Mm_Celera	X:151920527	TAGCAGAGGATTCTC[G/T]GCAGGTATAGGTTGG	59026
rs6173903	snp	C/T	0.5	0	intron-variant	Huwe1	Mm_Celera	X:151920655	GGTTTCTCTGTGTAG[C/T]CCTGGCTGTCCTGGA	59026
rs6174397	snp	A/G	0.5	0	intron-variant	Huwe1	Mm_Celera	X:151881922	ctattggatacatat[A/G]caaaataactctgta	59026
rs6174968	snp	C/T	0.5	0	intron-variant	Huwe1	Mm_Celera	X:151882045	cagcctatacatgaa[C/T]tgaacagagaaaaca	59026
rs6175569	snp	G/T	0.5	0	intron-variant	Huwe1	Mm_Celera	X:151882180	ggaagagcgtaaatg[G/T]tcagccctgaaaaat	59026
rs6189466	snp	A/G	0.260355	0.249785	intron-variant	Huwe1	Mm_Celera	X:151882411	AGAGGATAAAAGATA[A/G]GGTACAAGTGTATTA	59026
rs6207314	snp	A/G	0.290657	0.246672	synonymous-codon	Huwe1	Mm_Celera	X:151890062	AAAGAGAAGAGCCCA[A/G]ATGACTAAGGTATGT	59026
rs6221173	snp	C/T	0.5	0	intron-variant	Huwe1	GRCm38.p3	X:151890313	CAGTATTTTTGGAAC[C/T]ATTTGGTAAAGGCCT	59026
rs6222285	snp	A/T	0.359862	0.224567	intron-variant	Huwe1	Mm_Celera	X:151890552	GAAATTGTCATGGGT[A/T]TTTGGCTTGGAAAAA	59026
rs6258992	snp	C/T	0.290657	0.246672	intron-variant	Huwe1	Mm_Celera	X:151904700	GGTTTCTTTGATTTA[C/T]TTGGCTCTGATCATT	59026
rs13468346	snp	A/G			missense	Huwe1	Mm_Celera	X:151932558	TGACAGGAGCCATCC[A/G]CAAACAGCTGGCAGC	59026
rs13484064	snp	C/T	0.490978	0.0665555	intron-variant	Huwe1	GRCm38.p3	X:151897367	TAGAAATCACTTAGA[C/T]GAGTAAACAAATGTA	59026
rs29293644	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151899538	ACTTTAGAGTTATTA[A/G]TAGAAGTATCTCCTT	59026
rs29293645	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151899504	GGTGGTTTATAAATA[A/G]CATTGATATGACAAC	59026
rs29293646	snp	A/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151899454	TATTCGGTATCCTGC[A/T]TATAACTTACCCAAA	59026
rs29293647	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	GRCm38.p3	X:151899304	TCAAGTGTTTCATTA[A/G]ATTCCTTATACATTG	59026
rs29293648	snp	C/T	0.260355	0.249785	intron-variant	Huwe1	Mm_Celera	X:151898848	AATTTTTAGATTCTT[C/T]TTTATTTGAGTCATT	59026
rs29293649	snp	C/T	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151898802	CAAGGAAACAGTTGA[C/T]GAAATCTTTTGTATC	59026
rs29293650	snp	A/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151898779	ATGTGAAGCAATCAG[A/G]GTAACTGCAAGGAAA	59026
rs29293651	snp	A/G	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151898742	AATACTCATTGAAAG[A/G]AAAGCTAGTCTTTTC	59026
rs29293652	snp	C/T	0.231111	0.249285	synonymous-codon	Huwe1	Mm_Celera	X:151898634	AAACTACAGCTATAC[C/T]GTGGGCCAGTCTGAG	59026
rs29293653	snp	A/G	0.493827	0.0552116	intron-variant	Huwe1	GRCm38.p3	X:151898361	AAGTGGCCTAAAATG[A/G]AGAAATACTGTCTTC	59026
rs29293754	snp	A/T	0.152778	0.230321	intron-variant	Huwe1	GRCm38.p3	X:151861645	TGATCTGTAGTAACT[A/T]CACACTGAAACTCAA	59026
rs29293755	snp	A/T	0.486111	0.0821678	intron-variant	Huwe1	Mm_Celera	X:151861555	CAAAGGATGTTGCAC[A/T]TGCTTTTAGTTAAGT	59026
rs29293756	snp	A/G	0.5	0	intron-variant	Huwe1	GRCm38.p3	X:151861336	GCAATATGACCCAGT[A/G]TTTCCTTTTTTTAGT	59026
rs29293757	snp	A/G	0.142012	0.225474	intron-variant	Huwe1	Mm_Celera	X:151861068	GCATCACAAATGCAA[A/G]TTGGAACTCCATTTA	59026
rs29293758	snp	A/G	0.489796	0.070696	intron-variant	Huwe1	GRCm38.p3	X:151860586	TTTATTTACTACAGT[A/G]TAACATATTGCTACC	59026
rs29293759	snp	C/T	0.142012	0.225474	intron-variant	Huwe1	Mm_Celera	X:151860301	ACTGTTTTCTAAGAC[C/T]ACTTGGTTATCCAGA	59026
rs29293760	snp	A/G	0.260355	0.249785	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151859337	ACCTCCCTCTTAGCA[A/G]TAACATACAAAGTTG	59026
rs29293761	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151859248	TCATTCTATGTATCA[C/T]AGCCATCCTTCCCTA	59026
rs29293762	snp	G/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151859161	TTATTTCCTTTTCAT[G/T]TTCACATCTACAAGT	59026
rs29293763	snp	A/T	0.46875	0.121031	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151858914	GAAATTACATACTCA[A/T]TACAAAGAAAGTTAC	59026
rs29293764	snp	C/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151823330	AATTCTACCATTTTC[C/T]GAATGTAGATGTAGG	59026
rs29293765	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151823189	ATACTTGGAATTTGG[A/G]ACCTGAGATGATTTA	59026
rs29293766	snp	A/G	0.497041	0.0383476	intron-variant	Huwe1	Mm_Celera	X:151822921	TATTTTAAATACAGG[A/G]TATTGTTTGGCTTAT	59026
rs29293767	snp	A/G	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151822797	ATTGTTAGATACCAA[A/G]TAAGCACTACTTGAA	59026
rs29293768	snp	C/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151822745	ACATCAAGTCTCTAA[C/T]TGACATGTTTCAAAG	59026
rs29293769	snp	C/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151822064	TGTTCTGGATGTAAA[C/T]GAAATTTAAACTTCA	59026
rs29293770	snp	C/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151822052	GCTGTATACACTTGT[C/T]CTGGATGTAAACGAA	59026
rs29293771	snp	A/G	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151821641	TATCTACCCATGCAC[A/G]CAAGTTCTATTGAGT	59026
rs29293772	snp	A/C	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151821565	TCTGGTTTTTCACTT[A/C]CAAGTGGGTCCAGAA	59026
rs29293773	snp	A/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151821297	CAGTGAGTTTTGCTA[A/T]GTCATGCAGACTGGC	59026
rs29293973	snp	C/T	0.124444	0.216185	downstream-variant-500B	Huwe1	Mm_Celera	X:151935902	AAAAATTGTTGGGTC[C/T]ACAAGAGCTAGTTCT	59026
rs29294014	snp	C/T	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151898240	AAATTGCATAAACAT[C/T]AGGAAATAGTGGGTG	59026
rs29294015	snp	C/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151898107	TGAGATATAGAGAGA[C/G]CAATATTTCCATATG	59026
rs29294016	snp	A/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151898020	TATTGGATGCCTACC[A/T]ACAGCTTAAGAATTT	59026
rs29294017	snp	C/T	0.475309	0.108333	intron-variant	Huwe1	GRCm38.p3	X:151897878	TTTGGGGCATCTTTG[C/T]TCATACACATATCCA	59026
rs29294018	snp	C/T	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151897485	TGTCCTTTGGTTGTA[C/T]TATTTGTACTAGTCC	59026
rs29294019	snp	A/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151896470	CATAATTATTGCACT[A/G]GTACTCTTAAATGCA	59026
rs29294020	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151896305	TGGAATAACAACCAT[A/G]CTCTGTCAGTAATGA	59026
rs29294021	snp	A/G	0.484429	0.0868505	intron-variant	Huwe1	GRCm38.p3	X:151896299	TAATGTTGGAATAAC[A/G]ACCATGCTCTGTCAG	59026
rs29294022	snp	C/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151896168	GCTCTAATTGATGTA[C/G]CTATTGACTGGCCTC	59026
rs29294023	snp	A/C	0.48	0.0979796	intron-variant	Huwe1	Mm_Celera	X:151896060	ATAATAACTGTAGAA[A/C]AATGTGAGACTTTCA	59026
rs29294184	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151858610	TGTGCATGTTGCAGT[C/T]CACAGAAATCCTTTT	59026
rs29294185	snp	C/T	0.396694	0.202437	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151858169	AAACCTAATAAGCAC[C/T]GTGTAGTCAAAATAC	59026
rs29294186	snp	A/C	0.46875	0.121031	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151858155	TATTTACACTACTAA[A/C]ACCTAATAAGCACCG	59026
rs29294187	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151857996	TCTAATTCTTACTCA[C/T]AAATTAAAAGGCACA	59026
rs29294188	snp	A/G	0.49827	0.0293608	intron-variant, upstream-variant-2KB	Huwe1, Mir3113	Mm_Celera	X:151857939	AGTTATTAAGCCAAT[A/G]ATATTTCCATGTATG	59026
rs29294189	snp	C/T	0.18	0.24	intron-variant	Huwe1	Mm_Celera	X:151857402	ATTTTCGAAAAGCAA[C/T]ATTAATTTTTATAGC	59026
rs29294190	snp	C/G	0.142012	0.225474	intron-variant	Huwe1	Mm_Celera	X:151857332	ACATTCAGCATATGT[C/G]TTTATCTTCTCTCCA	59026
rs29294191	snp	C/T	0.132653	0.220748	synonymous-codon	Huwe1	Mm_Celera	X:151856775	TTTCTCCTTTTTGTA[C/T]CATCTGGCTAGCTAC	59026
rs29294192	snp	A/C	0.142012	0.225474	intron-variant	Huwe1	Mm_Celera	X:151856285	AAGTGGAGCCTGAAC[A/C]TTTTACTTTTTTCTT	59026
rs29294193	snp	C/G	0.132653	0.220748	intron-variant	Huwe1	Mm_Celera	X:151856022	TGTGCTGATTGGAAT[C/G]TGTGTTATACAGTGG	59026
rs29294194	snp	A/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151819218	TTCTTATCCCTGCCT[A/G]TAGACATTTTTTGAC	59026
rs29294195	snp	G/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151819114	GATTTAGCTGAGCAA[G/T]CCTCCCATGCCATTT	59026
rs29294196	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151818954	AGGCGCCTGGGGGGA[A/G]CATACACATTTTATC	59026
rs29294197	snp	A/G	0.48	0.0979796	intron-variant	Huwe1	Mm_Celera	X:151818022	AGAACCGAGTTTGGT[A/G]TTTGTGTAACTAGGT	59026
rs29294198	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151817944	TGGCACAGCTCTCAC[A/G]GCTGATCTGTGTAGC	59026
rs29294199	snp	A/T	0.244898	0.249948	intron-variant	Huwe1	Mm_Celera	X:151817111	TTTGGTTTTGCATTT[A/T]TGTGTATGTAAGTAA	59026
rs29294200	snp	A/G	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151816704	TGCCCCAAGTCCTGG[A/G]TTTGGTGTGAGCACT	59026
rs29294201	snp	A/T	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151816662	TTTCTGAACTGGGAA[A/T]GTAGTTCATTAGTGG	59026
rs29294202	snp	G/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151815930	TTCCTTTAAGCAACT[G/T]GCTTTTATTTCTAAA	59026
rs29294203	snp	A/G	0.142012	0.225474	intron-variant	Huwe1	Mm_Celera	X:151814586	TTATCAAAATCCTAC[A/G]CTTACATGTTTGTGT	59026
rs29294344	snp	C/T	0.244898	0.249948	utr-variant-3-prime, downstream-variant-500B	Huwe1	Mm_Celera	X:151934934	CTGAAAAAGAAAACC[C/T]CATCTTATACACATA	59026
rs29294345	snp	C/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151934206	AAGAAGCAGTGAGTA[C/G]ATGAGCTCTGGCTCA	59026
rs29294346	snp	C/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151933209	CTTCTAGACACCTAC[C/T]CAAGATTGGGAGCAC	59026
rs29294347	snp	C/T	0.124444	0.216185	synonymous-codon	Huwe1	Mm_Celera	X:151932724	GTACCAATCCAACTC[C/T]ATTCAGGTGAGCGGA	59026
rs29294348	snp	C/T	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151932062	CTAAGGCAGGCAGAT[C/T]TCTCAGTATAAGGTG	59026
rs29294349	snp	C/T	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151931577	AATTAGAATTACCCT[C/T]TTCTAACTTGTTTTA	59026
rs29294350	snp	A/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151931390	CATCTGTAACTCAAG[A/G]GTTGGAGGTACAAAG	59026
rs29294351	snp	C/G	0.5	0	intron-variant	Huwe1	GRCm38.p3	X:151929987	CACAGAATCTTTCTC[C/G]CTTACATGATGCTAC	59026
rs29294352	snp	G/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151929701	GTCTTTAATGCCTTT[G/T]CAGTGCAAGCTTAAT	59026
rs29294353	snp	C/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151929556	TAGCAGTGACCTAAT[C/G]TGGCCTCAAGTTTAG	59026
rs29294494	snp	A/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151895467	TAAAATACAAGAGGT[A/G]TGAGAATAATGGTGA	59026
rs29294495	snp	A/G	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151895439	ATACACACCTGAAGA[A/G]ACTTACTTACTATAA	59026
rs29294496	snp	A/G	0.487535	0.077957	intron-variant	Huwe1	GRCm38.p3	X:151895135	ATATTATCTCGCATG[A/G]ATCATTTCAGCTAGC	59026
rs29294497	snp	C/T	0.124444	0.216185	missense	Huwe1	Mm_Celera	X:151895014	CCTCATCTCTGCCTG[C/T]CATTCCTGATACTAT	59026
rs29294498	snp	A/G	0.345679	0.230967	intron-variant	Huwe1	Mm_Celera	X:151894359	GAAGTAATTACATTT[A/G]TATCAAATTATGGAA	59026
rs29294499	snp	A/T	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151893638	AGCATTTGCGGAGTC[A/T]TAGAGCCTACACTTA	59026
rs29294500	snp	A/C	0.124444	0.216185	intron-variant	Huwe1	Mm_Celera	X:151892979	GTTTAAGACCAGTTT[A/C]GCTGTTTAAGCTGTT	59026
rs29294501	snp	A/G	0.32	0.24	intron-variant	Huwe1	Mm_Celera	X:151892622	CATGATTGAATGAAG[A/G]GAATCTTTGAAAGAC	59026
rs29294502	snp	C/T	0.231111	0.249285	intron-variant	Huwe1	Mm_Celera	X:151892194	TGATGGGCCTTTAAC[C/T]ATTGTAAAAATTAGA	59026
rs29294503	snp	A/C/T	0.244898	0.249948	intron-variant	Huwe1	Mm_Celera	X:151892168	TTTAATGTTCCTGGT[A/C/T]TGTTGTGCACTGATG	59026
rs29294734	snp	C/T	0.297521	0.245442	intron-variant	Huwe1	Mm_Celera	X:151814344	CAAGGTGAGAGTTCA[C/T]AGTGATACATTCAAT	59026
rs29294735	snp	C/T	0.35503	0.226867	intron-variant	Huwe1	Mm_Celera	X:151813558	TTTGTACCCAGTCTC[C/T]ATTTTCCTTTTCCAC	59026
rs29294736	snp	G/T	0.497041	0.0383476	intron-variant	Huwe1	Mm_Celera	X:151813502	TGTGATAAGACAAAA[G/T]GTGAGATTGAAGGAA	59026
rs29294737	snp	G/T	0.260355	0.249785	intron-variant	Huwe1	Mm_Celera	X:151810958	CTGATTTCTCAGAGA[G/T]TGAAACACTTTACTC	59026
rs29294738	snp	C/T	0.277778	0.248452	intron-variant	Huwe1	Mm_Celera	X:151810735	AAGTTGAACTAAGTA[C/T]ATGAATCATTAATAG	59026
rs29294739	snp	A/C	0.277778	0.248452	intron-variant	Huwe1	Mm_Celera	X:151809895	CTCAGGTTTTAAGTT[A/C]TTAAAATTAAGCATA	59026

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